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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446062Generated: October 23, 2026

Water → 5-(3-Bromophenyl)-2-furaldehyde

https://huagongshe.com/en/reaction/446062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantBenzene, 1-bromo-3-iodo-HCID 11561—
Reactant5-Formylfuran-2-boronic acidHCID 2734355—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-(3-Bromophenyl)-2-furaldehydeHCID 84051725.9%

Reaction Steps

5-Formyl-2-furanboronic acid (676 mg, 4.8 mmol) and 3-bromoiodobenzene (1132 mg, 4 mmol) were dissolved in 1,2-dimethoxyethane (30 mL), tetrakis(triphenylphosphine)palladium (228 mg, 0.2 mmol) was added thereto, 2 mol/L sodium carbonate (9.6 mL) was further added thereto, and the mixture was heated to reflux for 2 hours while stirring. After the reaction was completed water (20 mL) was added thereto, and extraction with ethyl acetate (20 mL×2) was carried out. The organic layer was washed with saturated brine, water was removed using anhydrous sodium sulfate, the solvent was then removed by evaporation under reduced pressure, and the residue was subjected to silica gel column chromatography using ethyl acetate/hexane (3/7 (volume ratio)) as an eluent, to give 5-(3-bromophenyl)furan-2-carbaldehyde in a yield of 306 mg (yield 25.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476449B2
Source datasetuspto-grants-2013_07
ORD IDord-5e7c749d4a9446d4a9a263f8c69dd32d
Source noteuspto-grants-2013_07